CNRIP1 cannabinoid receptor interacting protein 1 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: CNRIP1provided by VGNC
Official Full Name: cannabinoid receptor interacting protein 1provided by VGNC
Primary source: VGNC:VGNC:106141
Locus tag: EGK_05392
See related: Ensembl:ENSMMUG00000046992
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 13

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	13	NC_041766.1 (40443704..40467392)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	13	NC_027905.1 (69365433..69389724, complement)

Chromosome 13 - NC_041766.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

D2S1627E (e-PCR)
- UniSTS:23309

RH18495 (e-PCR)
- UniSTS:57154

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables type 1 cannabinoid receptor binding	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in negative regulation of signaling receptor activity	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in plasma membrane	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: CB1 cannabinoid receptor-interacting protein 1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.